SODIUM ION BASED AQUEOUS ELECTROLYTE ELECTROCHEMICAL SECONDARY ENERGY STORAGE DEVICE

Description

FIELD OF THE INVENTION

[0001] The present invention is generally directed to a method of operating a hybrid aqueous energy storage device.

BACKGROUND OF THE INVENTION

[0002] Small renewable energy harvesting and power generation technologies (such as solar arrays, wind turbines, micro sterling engines, and solid oxide fuel cells) are proliferating, and there is a commensurate strong need for intermediate size secondary (rechargeable) energy storage capability. Batteries for these stationary applications typically store between 1 and 50 kWh of energy (depending on the application) and have historically been based on the lead-acid (Pb-acid) chemistry. Banks of deep-cycle lead-acid cells are assembled at points of distributed power generation and are known to last 1 to 10 years depending on the typical duty cycle. While these cells function well enough to support this application, there are a number of problems associated with their use, including: heavy use of environmentally unclean lead and acids (it is estimated that the Pb-acid technology is responsible for the release of over 100,000 tons of Pb into the environment each year in the US alone), significant degradation of performance if held at intermediate state of charge or routinely cycled to deep levels of discharge, a need for routine servicing to maintain performance, and the implementation of a requisite recycling program. There is a strong desire to replace the Pb-acid chemistry as used by the automotive industry. In this context, CN101241802 discloses a battery and a capacitor, and in particular an asymmetrical water-system sodium/potassium ion battery capacitor. Furthermore, WO2006/111079 discloses a lithium-based aqueous battery/supercapacitor electrical storage device, wherein a double layer capacitance is integrated with an intercalated mechanism to form a hybrid system. Finally, US5558961 discloses an alkali metal manganese oxide secondary cell which inter alia can provide a high rate of discharge, good cycling capabilities and high specific energy. The active material in the anode is an alkali metal and the active material in the cathode comprises a manganese oxide. Unfortunately the economics of alternative battery chemistries has made non-Pb-based solutions a very unappealing option to date.

[0003] Despite all of the recent advances in battery technologies, there are still no low-cost, clean alternates to the Pb-acid chemistry. This is due in large part to the fact that Pb-acid batteries are remarkably inexpensive compared to other chemistries (<$200/kWh), and there is currently a focus on developing higher-energy systems for transportation applications (which are inherently significantly more expensive than Pb-acid batteries).

SUMMARY OF THE INVENTION

[0004] Embodiments of the present invention provide a method according to claim 1 of operating a hybrid aqueous energy storage device comprising an anode electrode, a cathode electrode, a separator, and a sodium containing aqueous electrolyte, the method comprising deintercalating alkali ions from an active cathode electrode material during initial charging of the device, reversibly intercalating sodium ions into the active cathode electrode material during discharge cycles, and deintercalating sodium ions from the active cathode electrode during subsequent charge cycles.

[0005] As used herein, the term electronegativity is used to describe the ability of an atom to attract electrons in a covalent bond to itself. Several different scales may be used to describe electronegativity. Unless otherwise indicated, electronegativity values indicated herein are according to the Pauling scale.

[0006] As used herein, the term faradaic reaction indicates a reaction that results in oxidation or reduction of an involved species. For example, in embodiments of the present invention, when Na cations intercalate in to active cathode materials, the active cathode materials must be reduced (that is electrons must be transferred to the active cathode materials) in order to preserve electroneutrality of the bulk material. Conversely, nonfaradaic processes involve the accumulation of charge at the surface of an electrode/solution interface resulting in the formation of an electrical double layer.

[0007] As used herein, the term secondary energy storage device may be used interchangeably with the term secondary battery.

BRIEF DESCRIPTION OF THE DRAWINGS

[0008] 

Figure 1 shows an illustration of one possible charge/discharge mechanism employed by hybrid energy storage devices of the embodiments of the present invention.

Figure 2 shows a schematic representation of a secondary energy storage device according to an embodiment of the present invention.

Figure 3 shows the X-ray diffraction pattern obtained from spinel structure Li_1.05Mn_1.89Al_0.06O₄ synthesized according to the method described in Example 1 carried out in a test cell representative for the energy storage device described in the present invention.

Figure 4 shows the X-ray diffraction pattern obtained from spinel structure Mn_1.89Al_0.06O₄ (Al-doped λ-MnO₂) after deintercalation of Li from spinel Li_1.05Mn_1.89Al_0.06O₄ as described in Example 1.

Figures 5A and 5B show the overlap of a portion of the X-ray diffraction patterns from Figures 3 and 4.

Figure 6 shows data from three sequential cyclic voltammargrams for de-lithiated Al-doped λ-MnO₂ active cathode material in aqueous Na₂SO₄ electrolyte obtained after ten conditioning cycles.

Figure 7 shows cyclic voltammargram data for activated carbon anode material in aqueous Na₂SO₄ electrolyte. No distinct reduction-oxidation peaks are observed.

Figure 8 shows the charge/discharge behavior (i.e., cell potential versus time through charge/discharge cycles) of a full aqueous Na-ion hybrid energy storage device based on a de-lithiated Al-doped λ-MnO₂ active cathode material in aqueous Na₂SO₄ electrolyte at C/24 and 2C rates.

Figures 9A and 9B show single C/5 discharge behavior versus time and specific energy (Wh/kg), respectively, for Al-doped λ-MnO₂ active cathode material in aqueous Na₂SO₄ electrolyte from 1.7 to 0.8 V cell potential.

Figure 10 shows data from a single C/10 discharge cycle as a function of time for Al-doped λ-MnO₂ active cathode material in aqueous Na₂SO₄ electrolyte from 1.7 to 0.6 V cell potential.

Figures 11A and 11 B show data showing the cycling performance of Al-doped λ-MnO₂ active cathode material made via electrochemical Li/Na ion exchange in aqueous Na₂SO₄ electrolyte from 2.0 to 0.8 V cell potential.

Figures 12A and 12B show specific energy and specific capacity, respectively, versus cycle number for long term testing (up to 40 cycles) of a full aqueous Na-ion hybrid energy storage device based on a de-lithiated Al-doped λ-MnO₂ active cathode material in aqueous Na₂SO₄ electrolyte. Figure 12C shows extended high rate cycling performance (cell capacity versus cycle number) for more than 540 cycles at 5C rate across a potential range of 1.8 to 0.8 V.

Figure 13 shows the energy density as a function of cycle number for Al-doped λ-MnO₂ active cathode material in aqueous 1 M Na₂SO₄ electrolyte with C/5 cycling rate across a potential range of 1.9 to 0.8 V.

Figure 14 shows specific energy versus discharge rate for a cell with Al-doped λ-MnO₂ active cathode material versus activated carbon anode material in aqueous Na₂SO₄ electrolyte.

Figure 15 shows specific energy versus specific power for a cell with Al-doped λ-MnO₂ active cathode material versus activated carbon anode material in aqueous Na₂SO₄ electrolyte.

Figure 16 shows the temperature dependency of specific energy versus discharge rates for cells with Al-doped λ-MnO₂ active cathode material versus activated carbon anode material in aqueous Na₂SO₄ electrolyte.

Figure 17 shows long term cell capacity performance for a cell with Al-doped λ-MnO₂ active cathode material versus activated carbon anode material in aqueous Na₂SO₄ electrolyte over about 5000 cycles.

Figure 18 shows the cell potential versus cell energy for a two cell stack constructed with Al-doped λ-MnO₂ active cathode material versus activated carbon anode material in aqueous Na₂SO₄ electrolyte.

Figure 19 shows the charge/discharge behavior (i.e., cell potential versus time through charge/discharge cycles) of a full aqueous Na-ion hybrid energy storage device based on a NaMnO₂ (birnassite phase) active cathode material in aqueous Na₂SO₄ electrolyte.

Figure 20A shows data from four sequential cyclic voltammograms for Na₂Mn₃O₇ active cathode material in aqueous Na₂SO₄ electrolyte solution. Figure 20B shows a potential versus time profile from a portion of the cyclic voltammogram testing shown in Figure 20A.

Figure 21 shows discharge behavior of a test cell with a Na₂FePO₄F active cathode material, an activated carbon anode material, and aqueous Na₂SO₄ electrolyte.

Figure 22 shows a structural representation of the crystal structure of Na_0.44MnO₂ perpendicular to the ab plane.

Figure 23 shows a cyclic voltammogram of a composite Na_0.44MnO₂ electrode in an aqueous Na₂SO₄ electrolyte.

Figure 24 shows a cyclic voltammogram of a composite activated carbon electrode in an aqueous Na₂SO₄ electrolyte.

Figure 25 shows charge / discharge behavior of a composite Na_0.44MnO₂/Na₂SO₄ (aq)/ composite activated carbon hybrid electrical energy storage device through five cycles over about 15 hours.

Figure 26 shows specific capacity across a typical discharge cycle of a composite Na_0.44MnO₂/Na₂SO₄ (aq)/composite activated carbon hybrid electrical energy storage device.

Figure 27 shows long-term charge/discharge behavior of a composite Na_0.44MnO₂/Na₂SO₄ (aq)/composite activated carbon hybrid electrical energy storage device after 40 continuous hours of testing to about 60 continuous hours of testing.

Figure 28 shows a plot of charge and discharge capacity as a function of cycle for a composite Na_0.44MnO₂/Na₂SO₄ (aq)/composite activated carbon hybrid electrical energy storage device over 180 cycles.

Figure 29 shows a plot of charge and discharge energy as a function of cycle for a composite Na_0.44MnO₂/Na₂SO₄ (aq)/composite activated carbon hybrid electrical energy storage device over 110 cycles.

Figure 30A shows cell potential versus specific capacity for a full aqueous Na-ion hybrid energy storage device based on a composite Na_0.44MnO₂ cathode (made with hydrated NaMnO₂ (birnassite) as a binder) in aqueous Na₂SO₄ electrolyte. Figure 30B shows specific capacity versus cycle number for long term testing (over about 25 cycles) of a full aqueous Na-ion hybrid energy storage device based on a composite Na_0.44MnO₂ cathode (made with hydrated NaMnO₂ (birnassite) as a binder) in aqueous Na₂SO₄ electrolyte.

DETAILED DESCRIPTION OF THE INVENTION

[0009] Hybrid electrochemical energy storage systems of embodiments of the present invention include a double-layer capacitor electrode coupled with an active electrode. In these systems, the capacitor electrode stores charge through a reversible nonfaradiac reaction of Na cations on the surface of the electrode (double-layer), while the active electrode undergoes a reversible faradic reaction in a transition metal oxide that intercalates and deintercalates Na cations similar to that of a battery.

[0010] An example of a Li-based system has been described by Wang, et al., which utilizes a spinel structure LiMn₂O₄ battery electrode, an activated carbon capacitor electrode, and an aqueous Li₂SO₄ electrolyte. Wang, et al., Electrochemistry Communications, 7:1138-42 (2005). In this system, the negative anode electrode stores charge through a reversible nonfaradiac reaction of Li-ion on the surface of an activated carbon electrode. The positive cathode electrode utilizes a reversible faradiac reaction of Li-ion intercalation/deintercalation in spinel LiMn₂O₄.

[0011] In embodiments of the present invention, the charge/discharge processes of a device are associated with the transfer of Na cations between the active cathode electrode material and the anode electrode, with a Na cation containing electrolyte acting primarily as an ionic conductor between the two electrodes. That is, the cation concentration in the electrolyte stays relatively constant through a charge/discharge cycle. As the system is charged, cations in the electrolyte solution are adsorbed onto the surface of the anode material. At the same time, cations deintercalate from the active cathode material, thus keeping cation electrolyte concentration roughly constant through the charging process. Conversely, as the system is discharged, cations in the electrolyte solution intercalate into the active cathode material. At the same time, cations desorb from the surface of the anode material, thus keeping cation electrolyte concentration roughly constant through the discharge process. This process is shown schematically in Figure 1.

[0012] The highly-purified solvent-based non-aqueous electrolytes that must be used in energy storage devices, such as batteries, supercapacitors, or hybrid-energy storage systems, is a source of expense. Highly purified solvent-based non-aqueous electrolytes are typically necessary in Li-based systems because Li-ion systems are designed to have a relatively high operating potential, typically between about 3.3 and 4.2 V. Such high operating potentials are problematic for aqueous systems because water is electrolyzed at -1.3 V, so non-aqueous (i.e., solvent-based) electrolytes that are stable to >4 V are needed. This results in several undesirable consequences. First, the conductivity of these solvent-based electrolytes is much lower than water-based electrolytes, so Li-ion batteries are either significantly rate-limited, or must be fabricated in such a way that they have very thin porous electrodes. Usually the latter design is selected despite being a much more complicated design with high surface area current collectors, very thin roll-coated electrodes, and a large-area polymer separator. Much of the cost associated with state of the art Li-ion batteries is a result of this design paradigm. Second, the cost of handling and fabrication is elevated since a moisture-free environment must be maintained during battery assembly. Third, a controlled moisture-free fabrication environment is required, which also increases cost and complexity.

[0013] In contrast, embodiments of the present invention provide a secondary (rechargeable) energy storage system which uses a water-based (aqueous) electrolyte, such as a Na-based aqueous electrolyte. This allows for use of much thicker electrodes, much less expensive separator and current collector materials, and benign and more environmentally friendly materials for electrodes and electrolyte salts. Additionally, energy storage systems of embodiments of the present invention can be assembled in an open-air environment, resulting in a significantly lower cost of production.

[0014] Secondary (rechargeable) energy storage systems of embodiments of the present invention comprise an anode (i.e., negative) electrode, an anode side current collector, a cathode (i.e., positive) electrode, a cathode side current collector, a separator, and a Na-ion containing aqueous electrolyte. Any material capable of reversible intercalation/ deintercalation of Na-ions may be used as an active cathode material. Any material capable of reversible adsorption/desorption of Na-ions and can function together with such an active cathode material and an appropriate electrolyte solution may be used as an anode material. As shown in the schematic of an exemplary device in Figure 2, the cathode side current collector 1 is in contact with the cathode electrode 3. The cathode electrode 3 is in contact with the electrolyte solution 5, which is also in contact with the anode electrode 9. The separator 7 is located in the electrolyte solution 5 at a point between the cathode electrode 3 and the anode electrode 9. The anode electrode is also in contact with the anode side current collector 11. In Figure 2, the components of the exemplary device are shown as not being in contact with each other. The device was illustrated this way to clearly indicate the presence of the electrolyte solution relative to both electrodes. However, in actual embodiments, the cathode electrode 3 is in contact with the separator 7, which is in contact with the anode electrode 9.

Device Components

Cathode

[0015]  Materials that may be used as cathodes in the present invention comprise materials that do not contain Na in an as-formed state, but are capable of reversible intercalation/deintercalation of Na-ions during discharging/ charging cycles of the energy storage device without a large overpotential loss.

[0016] The active cathode material contains lithium atoms prior to use, some or all of these atoms are deintercalated during the first cell charging cycle. Alkali cations from the electrolyte (overwhelmingly Na cations) are re-intercalated during cell discharge. This is different than nearly all of the hybrid capacitor systems that call out an intercalation electrode opposite activated carbon. In most systems, cations from the electrolyte are adsorbed on the anode during a charging cycle. At the same time, the counter-anions, such as hydrogen ions, in the electrolyte intercalate into the active cathode material, thus preserving charge balance, but depleting ionic concentration, in the electrolyte solution. During discharge, cations are released from the anode and anions are released from the cathode, thus preserving charge balance, but increasing ionic concentration, in the electrolyte solution. This is a different operational mode from devices in embodiments of the present invention, where hydrogen ions or other anions are preferably not intercalated into the cathode active material.

[0017] Suitable active cathode materials include λ-MnO₂ based material, e.g., Li_xM₂O₄ (where 1 ≤ x < 1.1) before use and Na_yMn₂O₄ in use).

[0018] In the cubic spinel λ-MnO₂ active cathode material, most or all of the Li is extracted electrochemically from the cubic spinel LiMn₂O₄ to form cubic spinel λ-MnO₂ type material (i.e., material which has a 1:2 Mn to O ratio, and/or in which the Mn may be substituted by another metal, and/or which also contains an alkali metal, and/or in which the Mn to O ratio is not exactly 1:2). This extraction takes place as part of the initial device charging cycle. In such instances, Li-ions are deintercalated from the as-formed cubic spinel LiMn₂O₄ during the first charging cycle. Upon discharge, Na-ions from the electrolyte intercalate into the cubic spinel λ-MnO₂. As such, the formula for the active cathode material during operation is Na_yLi_xMn₂O₄ (optionally doped with one or more additional metal as described above, preferably Al), with 0 < x < 1, 0 < y < 1, and x + y ≤ 1.1. Preferably, the quantity x + y changes through the charge/discharge cycle from about 0 (fully charged) to about 1 (fully discharged). However, values above 1 during full discharge may be used. Furthermore, any other suitable formation method may be used. Nonstoichiometric Li_xMn₂O₄ materials with more than 1 Li for every 2 Mn and 4 O atoms may be used as initial materials from which cubic spinel λ-MnO₂ may be formed (where 1 ≤ x < 1.1 for example). Thus, the cubic spinel A-manganate may have a formula Al_zLi_xMn_2-zO₄ where 1 ≤ x < 1.1 and 0 ≤ z < 0.1 before use, and Al_zLi_xMn₂O₄ where 0 ≤ x < 1.1, 0 ≤ x < 1, 0 ≤ x+y < 1.1, and 0 ≤ z < 0.1 in use (and where Al may be substituted by another dopant).

[0019] Optionally, the cathode electrode may be in the form of a composite cathode comprising one or more active cathode materials, a high surface area conductive diluent (such as conducting grade graphite, carbon blacks, such as acetylene black, non-reactive metals, and/or conductive polymers), a binder, a plasticizer, and/or a filler. Exemplary binders may comprise polytetrafluoroethylene (PTFE), a polyvinylchloride (PVC)-based composite (including a PVC-SiO₂ composite), cellulose-based materials, polyvinylidene fluoride (PVDF), hydrated birnassite (when the active cathode material comprises another material), other non-reactive non-corroding polymer materials, or a combination thereof. A composite cathode may be formed by mixing a portion of one or more preferred active cathode materials with a conductive diluent, and/or a polymeric binder, and pressing the mixture into a pellet. In some embodiments, a composite cathode electrode may be formed from a mixture of about 50 to 90 wt% active cathode material, with the remainder of the mixture comprising a combination of one or more of diluent, binder, plasticizer, and/or filler. For example, in some embodiments, a composite cathode electrode may be formed from about 80 wt% active cathode material, about 10 to 15 wt% diluent, such as carbon black, and about 5 to 10 wt% binder, such as PTFE.

[0020] One or more additional functional materials may optionally be added to a composite cathode to increase capacity and replace the polymeric binder. These optional materials include but are not limited to Zn, Pb, hydrated NaMnO₂ (birnassite), and hydrated Na_0.44MnO₂ (orthorhombic tunnel structure). In instances where hydrated NaMnO₂ (birnassite) and/or hydrated Na_0.44MnO₂ (orthorhombic tunnel structure) is added to a composite cathode, the resulting device has a dual functional material composite cathode.

[0021] A cathode electrode will generally have a thickness in the range of about 40 to 800 µm.

Anode:

[0022] The anode may comprise any material capable of reversibly storing Na-ions through surface adsorption/desorption (via an electrochemical double layer reaction and/or a pseudocapacitive reaction (i.e., a i.e. partial charge transfer surface interaction)) and have sufficient capacity in the desired voltage range. Exemplary materials meeting these requirements include porous activated carbon, graphite, mesoporous carbon, carbon nanotubes, disordered carbon, Ti-oxide (such as titania) materials, V-oxide materials, phospho-olivine materials, other suitable mesoporous ceramic materials, and a combinations thereof. In preferred embodiments, activated carbon is used as the anode material.

[0023] Optionally, the anode electrode may be in the form of a composite anode comprising one or more anode materials, a high surface area conductive diluent (such as conducting grade graphite, carbon blacks, such as acetylene black, non-reactive metals, and/or conductive polymers), a binder, such as PTFE, a PVC-based composite (including a PVC-SiO₂ composite), cellulose-based materials, PVDF, other non-reactive non-corroding polymer materials, or a combination thereof, plasticizer, and/or a filler. A composite anode may be formed my mixing a portion of one or more preferred anode materials with a conductive diluent, and/or a polymeric binder, and pressing the mixture into a pellet. In some embodiments, a composite anode electrode may be formed from a mixture from about 50 to 90 wt% anode material, with the remainder of the mixture comprising a combination of one or more of diluent, binder, plasticizer, and/or filler. For example, in some embodiments, a composite cathode electrode may be formed from about 80 wt% activated carbon, about 10 to 15 wt% diluent, such as carbon black, and about 5 to 10 wt% binder, such as PTFE.

[0024] One or more additional functional materials may optionally be added to a composite anode to increase capacity and replace the polymeric binder. These optional materials include but are not limited to Zn, Pb, hydrated NaMnO₂ (birnassite), and hydrated Na_0.44MnO₂ (orthorhombic tunnel structure).

[0025] An anode electrode will generally have a thickness in the range of about 80 to 1600 µm.

Current Collectors:

[0026] In embodiments of the present invention, the cathode and anode materials may be mounted on current collectors. For optimal performance, current collectors are desirable that are electronically conductive and corrosion resistant in the electrolyte (aqueous Na-cation containing solutions, described below) at operational potentials.

[0027] For example, an anode current collector must be stable in a range of approximately - 1.2 to -0.5 V vs. a standard Hg/Hg₂SO₄ reference electrode, since this is the nominal potential range that the anode half of the electrochemical cell is exposed during use. A cathode current collector must be stable in a range of approximately 0.1 to 0.7 V vs. a standard Hg/Hg₂SO₄ reference electrode.

[0028] Suitable uncoated current collector materials for the anode side include stainless steel, Ni, Ni-Cr alloys, Al, Ti, Cu, Pb and Pb alloys, refractory metals, and noble metals.

[0029] Suitable uncoated current collector materials for the cathode side include stainless steel, Ni, Ni-Cr alloys, Ti, Pb-oxides (PbOx), and noble metals.

[0030] Current collectors may comprise solid foils or mesh materials.

[0031] Another approach is to coat a metal foil current collector of a suitable metal, such as Al, with a thin passivation layer that will not corrode and will protect the foil onto which it is deposited. Such corrosion resistant layers may be, but are not limited to, TiN, CrN, C, CN, NiZr, NiCr, Mo, Ti, Ta, Pt, Pd, Zr, W, FeN, CoN, etc. These coated current collectors may be used for the anode and/or cathode sides of a cell. In one embodiment, the cathode current collector comprises Al foil coated with TiN, FeN, C, or CN. The coating may be accomplished by any method known in the art, such as but not limited to physical vapor deposition such as sputtering, chemical vapor deposition, electrodeposition, spray deposition, or lamination.

Electrolyte:

[0032] Electrolytes useful in embodiments of the present invention comprise a salt dissolved fully in water. For example, the electrolyte may comprise a 0.1 M to 10 M solution of at least one anion selected from the group consisting of SO₄^2-, NO^3-, ClO^4-, PO₄^3-, CO₃^2-, Cl^-, and/or OH^-. Thus, Na cation containing salts may include (but are not limited to) Na₂SO₄, NaNO₃, NaClO₄, Na₃PO₄, Na₂CO_3, NaCl, and NaOH, or a combination thereof.

[0033] Molar concentrations preferably range from about 0.05 M to 3 M, such as about 0.1 to 1 M, at 100°C for Na₂SO₄ in water depending on the desired performance characteristics of the energy storage device, and the degradation/performance limiting mechanisms associated with higher salt concentrations. Similar ranges are preferred for other salts.

[0034] A blend of different salts (such as a blend of a sodium containing salt with one or more of an alkali, alkaline earth, lanthanide, aluminum and zinc salt) may result in an optimized system. Such a blend may provide an electrolyte with sodium cations and one or more cations selected from the group consisting of alkali (such as K), alkaline earth (such as Mg and Ca), lanthanide, aluminum, and zinc cations.

[0035] Optionally, the pH of the electrolyte may be altered by adding some additional OH-ionic species to make the electrolyte solution more basic, for example by adding NaOH other OH-containing salts, or by adding some other OH- concentration-affecting compound (such as H₂SO₄ to make the electrolyte solution more acidic). The pH of the electrolyte affects the range of voltage stability window (relative to a reference electrode) of the cell and also can have an effect on the stability and degradation of the active cathode material and may inhibit proton (H+) intercalation, which may play a role in active cathode material capacity loss and cell degradation. In some cases, the pH can be increased to 11 to 13, thereby allowing different active cathode materials to be stable (than were stable at neutral pH 7). In some embodiments, the pH may be within the range of about 3 to 13, such as between about 3 and 6 or between about 8 and 13.

[0036] Optionally, the electrolyte solution contains an additive for mitigating degradation of the active cathode material, such as birnassite material. An exemplary additive may be, but is not limited to, Na₂HPO₄, in quantities sufficient to establish a concentration ranging from 0.1 mM to 100 mM.

Separator:

[0037] A separator for use in embodiments of the present invention may comprise a cotton sheet, PVC (polyvinyl chloride), PE (polyethylene), glass fiber or any other suitable material.

Operational Characteristics

[0038] As described above some or all of the lithium atoms are deintercalated during the first cell charging cycle. Alkali cations from the electrolyte (overwhelmingly Na cations) are re-intercalated during cell discharge. This is different than nearly all of the hybrid capacitor systems that call out an intercalation electrode opposite activated carbon. In most systems, cations from the electrolyte are adsorbed on the anode during a charging cycle. At the same time, the counter-anions in the electrolyte intercalate into the active cathode material, thus preserving charge balance, but depleting ionic concentration, in the electrolyte solution. During discharge, cations are released from the anode and anions are released from the cathode, thus preserving charge balance, but increasing ionic concentration, in the electrolyte solution. This is a different operational mode from devices in embodiments of the present invention.

[0039] In some embodiments, a hybrid energy storage device according to an embodiment of the present invention may be capable of operating over 500 cycles, such as over 5000 cycles, such as between 5000 and 10000 cycles at full discharge with less than 20% loss of initial capacity; preferably less than or equal to 10% loss of initial capacity; preferably less than or equal to about 5% loss of initial capacity, such as between 0 and 10 % loss of initial capacity; such as between 1 and 5 %.

[0040] In some embodiments, a hybrid energy storage device according to an embodiment of the present invention comprises an activated carbon anode material exhibiting greater than or equal to about 60 mAh/g specific capacity (cathode basis), such as 60 to 130 mAh/g (cathode basis), with Na₂SO₄ electrolyte.

[0041] The following example serve to illustrate the invention. The Example is in no way intended to limit the scope of the claimed method.

EXAMPLES

Example 1

[0042] A test cell was constructed with a λ-MO₂-type active cathode material versus an activated carbon anode material in 1 M Na₂SO₄ in Dl H₂O electrolyte.

[0043] The active cathode material was made from Al-doped, Li containing, cubic spinel MnO₂. Specifically, the Li-containing cubic spinel was synthesized by thoroughly mixing Li₂CO₃, Mn₂O₃, and Al(OH)₃ to proper mole ratios and firing at 750°C for 24 hours. This material resulted in a spinel structure with the formula Li_1.05Mn_1.89Al_0.06O₄, as verified by X-ray diffraction analysis. X-ray spectra is shown in Figure 3. As the X-ray data confirm, this material fits the well known cubic spinel LiMn₂O₄ structure, as archived by JCPDS card # 00-035-0782.

[0044] A composite cathode was formed by mixing about 80 wt% Li_1.05Mn_1.89Al_0.06O₄ initial active material, 10 wt% carbon black conductive diluent, and about 10% PTFE polymeric binder. This mixture was then pressed into a pellet, which was placed into a large electrochemical cell and biased to remove most of the Li. The cell was held at greater than 4.1 V for at least 5 hours to electrochemically extract the Li, although chemical extraction could have been used instead.

[0045] Once the electrochemical extraction was completed, X-ray diffraction analysis was again performed on the pellet, and a new Al-doped λ-MnO₂ phase was indicated that was substantially free of Li (i.e., 0 to 5 at% Li may have remained). The diffraction pattern from the new phase is shown in Figure 3.

[0046] The data in Figure 4 show that the material is a close match to λ-MnO₂ as described by JCPDS card # 00-044-0992. The diffraction patterns shown in Figures 3 and 4 are superimposed in Figure 5 to demonstrate the difference.

[0047] The resulting Al-doped A-MnO₂ material was then placed as a working electrode (cathode) into an electrochemical half cell environment with a Pt counter electrode, and a mercury/mercury sulfate reference electrode, and a Na₂SO₄ aqueous electrolyte. The half-cell was cycled between -0.3 and 0.6 V vs. SME. The data indicate that the cathode does display Na-ion intercalation/deintercalation events and is stable over many cycles. The data shown in Figure 6 show three sequential cyclic voltammargrams obtained after ten conditioning cycles. This result indicates that Al-doped λ-MnO₂ is able to reversibly intercalate Na cations from a Na cation containing electrolyte with virtually no Li or Li cations present.

[0048] To make a functional cell, a pellet was pressed of the composite Li-containing active cathode material described above and placed in a coin cell. The anode, separator, and electrolyte in the coin cell are described below.

[0049] Activated carbon was used as the anode material. This material is known to reversibly store Li cations through surface adsorption/desorption and also has sufficient capacity in the desired voltage range. It was anticipated that this material could store between 40 and 100 mAh/g of Na⁺ in the voltage range of 1.5 to 2 V vs. Na metal.

[0050] A composite anode was formed by mixing about 80 wt% activated carbon, 10 wt% carbon black conductive diluent, and 10 wt% PTFE polymeric binder and pressing the mixture into a pellet. The density of the pellet was at least 0.35 g/cm³. The mass of the pressed anode pellet was matched to the mass of the cathode pellet so that both electrodes could hold sufficient Na cations to make maximum use of the active material present.

[0051] This composite anode material was placed as a working electrode into an electrochemical half cell environment with a Pt counter electrode, and a mercury/mercury sulfate reference electrode. The half-cell was cycled between -0.6 and 0.7 V vs. SME, with a 1 M Na₂SO₄ electroty solution. The data indicate that the anode material does not display Na-ion intercalation/deintercalation events, exhibited symmetrical behavior indicative of a reversible Na cation storage process via a surface adsorption/electrochemical double layer capacitance effect. A cyclic voltammargram obtained from this half cell is shown in Figure 7.

[0052] The anode and cathode material pellets were fitted into standard stainless steel 2032 coin cell test fixtures. Cotton sheeting was used as a separator material, and Ni mesh served a current collectors for both electrodes. After some irreversible capacity loss on the first several formation cycles, typical charge/discharge behavior was observed to be very consistent and stable in the voltage range between 0.8 and 1.8 V, at least, as shown in Figure 8. The cell delivered uniform charge/discharge behavior during both C/24 and 2 C cycling and little obvious decay was observed.

[0053] Data showing a single C/5 discharge curve as a function of time and as a function of specific energy are shown in Figures 9A and 9B, respectively. Data showing a single C/10 discharge curve as a function of specific energy is shown in Figure 10.

[0054] Further study indicated that the cells are stable and can be cycled repeatedly between 1.8 and 0.8 V, at least. The cells also exhibit excellent long-term stability. Figures 12A and 12B show specific energy and specific capacity, respectively, versus cycle number for long term testing (up to 40 cycles). After the formation cycling is complete, a near-100% columbic efficiency is observed. Figure 12C shows extended high rate cycling performance, with little cell capacity degradation observed over 570 cycles at 5°C. As seen in Figure 17, such cells exhibit little to no degradation for 1000 or more charge/discharge cycles and less than 10% degradation over 5000 or more cycles, such as 5000 to 10,000 cycles.

[0055] Figure 13 shows the energy density of such cells as a function of cycle number, Figure 14 shows the specific energy versus discharge rate, and Figure 15 shows the specific energy versus specific power. Finally, temperature dependency studies were conducted. Figure 16 shows the temperature dependency of the specific energy versus discharge rates for a cell with this active cathode material.

[0056] Additionally, a large scale cell (i.e., a two cell stack) was constructed with the active cathode material composite electrode versus an activated carbon anode electrode. The cell potential versus the cell energy is shown in Figure 18.

[0057] A separate test cell was constructed from a fully de-lithiated, Al doped cubic spinel active cathode material (where Li was removed in a half cell environment described above and replaced with Na electrochemically in a half cell before assembling in the test cell) to demonstrate that this material is fully functional as an active cathode material. Cell cycle characteristics for this cell are shown in Figures 11A and 11 B. The cell showed significant capacity and a similar characteristic charge discharge profile as the cell where the starting material was Al doped LiMn₂O₄, described above.

[0058] In the processing of the above active cathode material, Li could have been removed chemically with a Br containing solution followed by washing. Additionally, Na could have also been added to a de-lithiated, cubic spinel active cathode material chemically by treatment with molten Na salt or Na containing solution.

[0059] The foregoing description of the invention has been presented for purposes of illustration and description. The method illustratively described herein may suitably be practiced in the absence of any element or elements, limitation or limitations, not specifically disclosed herein. Thus, for example, the terms "comprising", "including," containing", etc. shall be read expansively and without limitation. Additionally, the terms and expressions employed herein have been used as terms of description and not of limitation, and there is no intention in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the invention embodied therein herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention. It is intended that the scope of the invention be defined by the claims appended hereto.

Claims

1. A method of operating a hybrid aqueous energy storage device comprising an anode electrode, a cathode electrode, a separator, and a sodium containing aqueous electrolyte, the method comprising:

providing the storage device in which the cathode electrode comprises an active cathode electrode material comprising lithium λ-manganate cubic spinel material having a formula LiMn₂O₄,

deintercalating lithium ions from the active cathode electrode material during initial charging of the device, to form a substantially lithium free cubic spinel λ-manganate active cathode electrode material,

reversibly intercalating sodium ions into the active cathode electrode material during a subsequent discharge cycle to form a cubic spiel λ-manganate active cathode electrode material having a formula Na_yLi_xMn₂O₄ with 0<x<1, 0<y<1, and x+y≤1.1,

wherein at least 80 atomic percent of the alkaline metal is Na, and

reversibly deintercalating sodium ions from the active cathode electrode during subsequent charge cycles.

2. The method of claim 1, wherein a cation concentration of the electrolyte is substantially constant during the discharge and charge cycles of the device.

3. The method of claim 2, wherein the device exhibits a specific energy of greater than 20 Wh per kg of active cathode material when cycled between potentials of 0.60 and 1.9 V in 1 M Na₂SO₄ at C/10 rate or slower.

4. The method of claim 2, wherein the anode electrode comprises porous activated carbon, graphite, mesoporous carbon, carbon nanotubes, disordered carbon, Ti-oxide material, V-oxide material, phospho-olivine material, mesoporous ceramic material or a composite thereof, and the electrolyte comprises Na₂SO₄, NaNO₃, NaClO₄ Na₃PO₄, Na₂CO₃, NaCl, NaOH, or combination thereof, and the anode electrode is a double-layer capacitor electrode which stores charge through a reversible nonfaradiac reaction of alkali metal cations on a surface of the anode electrode or a pseudocapacitive electrode which undergoes a partial charge transfer surface interaction with alkali metal cations on a surface of the anode electrode.

Ansprüche

1. Verfahren zum Betreiben einer hybriden wässrigen Energiespeichervorrichtung, umfassend eine Anodenelektrode, eine Kathodenelektrode, einen Separator und ein Natrium enthaltendes wässriges Elektrolyt, wobei das Verfahren umfasst:

Bereitstellen der Speichervorrichtung, in welcher die Kathodenelektrode ein aktives Kathodenelektrodenmaterial mit Lithium A-Manganat-Kubikspinellmaterial mit einer Formel LiMn₂O₄ umfasst,

Deinterkalieren der Lithiumionen aus dem aktiven Kathodenelektrodenmaterial während der anfänglichen Ladung der Vorrichtung, um ein im Wesentlichen Lithium-freies kubisches Spinell- λ-Manganat als aktives Kathodenelektrodenmaterial zu bilden,

reversibles Interkalieren von Natriumionen in das aktive Kathodenelektrodenmaterial während eines nachfolgenden Entladezyklus, um ein kubisches Spinell- λ-Manganat als aktives Kathodenelektrodenmaterial mit einer Formel Na_yLi_xMn₂O₄, wobei 0<x<1, 0<y<1 und x+y≤1, 1, zu bilden,

wobei zumindest 80 Atom-% des Alkalimetalls Na ist, und reversibles Deinterkalieren von Natriumionen aus der aktiven Kathodenelektrode während nachfolgender Ladezyklen.

2. Verfahren nach Anspruch 1, wobei eine Kationenkonzentration des Elektrolyts während der Entlade- und Ladezyklen der Vorrichtung im Wesentlichen konstant ist.

3. Verfahren nach Anspruch 2, wobei die Vorrichtung eine spezifische Energie größer als 20 Wh pro kg aktives Kathodenmaterial aufweist, bei Zyklen zwischen Potentialen von 0,60 und 1,9 V in 1M Na₂SO₄ bei einer C10-Rate oder langsamer.

4. Verfahren nach Anspruch 2, wobei die Anodenelektrode poröse Aktivkohle, Graphit, mesoporöse Kohle, Kohlenstoff-Nanoröhrchen, ungeordneten Kohlenstoff, Ti-Oxid-Material, V-Oxid-Material, Phospho-Olivin-Material, mesoporöses Keramikmaterial oder eine Mischung aus diesen umfasst, und das Elektrolyt Na₂SO₄, NaNO₃, NaClO₄, Na₃PO₄, Na₂CO₃, NaCl, NaOH oder eine Kombination aus diesen umfasst, und die Anodenelektrode eine Doppelschicht-Kondensatorelektrode ist, welche eine Ladung durch eine reversible nichtfaradische Reaktion von Alkalimetallkationen auf einer Oberfläche der Anodenelektrode oder einer pseudokapazitiven Elektrode, welche eine teilweise Ladungsübertragungs-Oberflächeninteraktion mit Alkalimetallkationen auf einer Oberfläche der Anodenelektrode erfährt, speichert.

Revendications

1. Procédé d'exploitation d'un dispositif de stockage d'énergie aqueux hybride comprenant une électrode anode, une électrode cathode, un séparateur, et un électrolyte aqueux contenant du sodium, le procédé comprenant :

la fourniture du dispositif de stockage dans lequel l'électrode cathode comprend un matériau d'électrode cathode actif comprenant un matériau de spinelle cubique λ-manganate de lithium répondant à la formule LiMn₂O₄,

la désintercalation d'ions lithium du matériau d'électrode cathode actif durant une charge initiale du dispositif, pour former un matériau d'électrode cathode actif λ-manganate de spinelle cubique sensiblement dépourvu de lithium,

l'intercalation réversible d'ions sodium dans le matériau d'électrode cathode actif pendant un cycle de décharge ultérieur pour former un matériau d'électrode de cathode actif λ-manganate de spinelle cubique répondant à la formule Na_yLi_xMn₂O₄ avec 0 < x < 1, 0 < y < 1, et x + y ≤ 1,1, dans lequel au moins 80 pour cent atomique du métal alcalin est Na, et la désintercalation réversible d'ions sodium de l'électrode cathode active durant des cycles de charge ultérieurs.

2. Procédé selon la revendication 1, dans lequel une concentration en cation de l'électrolyte est sensiblement constante durant les cycles de décharge et charge du dispositif.

3. Procédé selon la revendication 2, dans lequel le dispositif affiche une énergie spécifique de plus de 20 Wh par kg de matériau de cathode actif lorsqu'il est cyclé entre des potentiels de 0,60 et 1,9 V dans du Na₂SO₄ à 1 M à une cadence de C/10 ou plus lente.

4. Procédé selon la revendication 2, dans lequel l'électrode anode comprend du charbon actif poreux, du graphite, du carbone mésoporeux, des nanotubes de carbone, du carbone désordonné, un matériau oxyde de Ti, un matériau oxyde de V, un matériau phospho-olivine, un matériau céramique mésoporeux ou un composite de ceux-ci, et l'électrolyte comprend Na₂SO₄, NaNO₃, NaClO₄, Na_sPO₄, Na₂CO₃, NaCl, NaOH, ou l'une de leur combinaison, et l'électrode anode est une électrode de condensateur double couche qui stocke une charge par une réaction non faradique réversible de cations de métal alcalin sur une surface de l'électrode anode ou une électrode pseudocapacitive qui subit une interaction de surface de transfert de charge partiel avec des cations de métal alcalin sur une surface de l'électrode anode.

Drawing